ATP13A1
Endoplasmic reticulum transmembrane helix translocase
Also known as: AT131_HUMAN, ATP13A, CGI-152, FLJ31858, KIAA1825
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HD20
- Gene
- ATP13A1
- Ensembl
- ENSG00000105726
- Chromosome
- 19
- Canonical length
- 1204 aa
- Protein class
- Plasma proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
Enables membrane protein dislocase activity. Involved in extraction of mislocalized protein from ER membrane. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1204 residues, UniProt reviewed canonical sequence.
>Q9HD20|ATP13A1
1 MAAAAAVGNA VPCGARPCGV RPDGQPKPGP QPRALLAAGP ALIANGDELV AAVWPYRRLA
61 LLRRLTVLPF AGLLYPAWLG AAAAGCWGWG SSWVQIPEAA LLVLATICLA HALTVLSGHW
121 SVHAHCALTC TPEYDPSKAT FVKVVPTPNN GSTELVALHR NEGEDGLEVL SFEFQKIKYS
181 YDALEKKQFL PVAFPVGNAF SYYQSNRGFQ EDSEIRAAEK KFGSNKAEMV VPDFSELFKE
241 RATAPFFVFQ VFCVGLWCLD EYWYYSVFTL SMLVAFEASL VQQQMRNMSE IRKMGNKPHM
301 IQVYRSRKWR PIASDEIVPG DIVSIGRSPQ ENLVPCDVLL LRGRCIVDEA MLTGESVPQM
361 KEPIEDLSPD RVLDLQADSR LHVIFGGTKV VQHIPPQKAT TGLKPVDSGC VAYVLRTGFN
421 TSQGKLLRTI LFGVKRVTAN NLETFIFILF LLVFAIAAAA YVWIEGTKDP SRNRYKLFLE
481 CTLILTSVVP PELPIELSLA VNTSLIALAK LYMYCTEPFR IPFAGKVEVC CFDKTGTLTS
541 DSLVVRGVAG LRDGKEVTPV SSIPVETHRA LASCHSLMQL DDGTLVGDPL EKAMLTAVDW
601 TLTKDEKVFP RSIKTQGLKI HQRFHFASAL KRMSVLASYE KLGSTDLCYI AAVKGAPETL
661 HSMFSQCPPD YHHIHTEISR EGARVLALGY KELGHLTHQQ AREVKREALE CSLKFVGFIV
721 VSCPLKADSK AVIREIQNAS HRVVMITGDN PLTACHVAQE LHFIEKAHTL ILQPPSEKGR
781 QCEWRSIDGS IVLPLARGSP KALALEYALC LTGDGLAHLQ ATDPQQLLRL IPHVQVFARV
841 APKQKEFVIT SLKELGYVTL MCGDGTNDVG ALKHADVGVA LLANAPERVV ERRRRPRDSP
901 TLSNSGIRAT SRTAKQRSGL PPSEEQPTSQ RDRLSQVLRD LEDESTPIVK LGDASIAAPF
961 TSKLSSIQCI CHVIKQGRCT LVTTLQMFKI LALNALILAY SQSVLYLEGV KFSDFQATLQ
1021 GLLLAGCFLF ISRSKPLKTL SRERPLPNIF NLYTILTVML QFFVHFLSLV YLYREAQARS
1081 PEKQEQFVDL YKEFEPSLVN STVYIMAMAM QMATFAINYK GPPFMESLPE NKPLVWSLAV
1141 SLLAIIGLLL GSSPDFNSQF GLVDIPVEFK LVIAQVLLLD FCLALLADRV LQFFLGTPKL
1201 KVPSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATP13A1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 10
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- spleen: 25 nTPM
- parathyroid gland: 22 nTPM
- small intestine: 21 nTPM
- appendix: 21 nTPM
- ovary: 20 nTPM
- lymph node: 20 nTPM
Single-cell type
- plasma cells: 37 nCPM
- respiratory ciliated cells: 28 nCPM
- colonocytes: 27 nCPM
- enterocytes: 27 nCPM
- cardiomyocytes: 26 nCPM
- fallopian tube ciliated cells: 25 nCPM
Immune cell
- non-classical monocyte: 8.6 nTPM
- myeloid DC: 6.5 nTPM
- intermediate monocyte: 5.6 nTPM
- plasmacytoid DC: 5 nTPM
- classical monocyte: 3.5 nTPM
- eosinophil: 3.5 nTPM
Brain region
- choroid plexus: 34 nTPM
- white matter: 26 nTPM
- hypothalamus: 25 nTPM
- medulla oblongata: 25 nTPM
- thalamus: 24 nTPM
- cerebral cortex: 24 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.29
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 2.66
- DepMap mean gene effect
- -0.23
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular calcium ion homeostasis
- monoatomic ion transmembrane transport
- protein transport
- transmembrane transport
- extraction of mislocalized protein from ER membrane
Molecular functions
- ATP binding
- ATP hydrolysis activity
- ATPase-coupled monoatomic cation transmembrane transporter activity
- membrane protein dislocase activity
- metal ion binding
- P-type ion transporter activity
- ABC-type manganese transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- P-type ATPase
- P-type ATPase, subfamily V
- P-type ATPase, A domain superfamily
- P-type ATPase, phosphorylation site
- HAD superfamily
- P-type ATPase, transmembrane domain superfamily
- P-type ATPase, cytoplasmic domain N
- HAD-like superfamily
- P-type ATPase, haloacid dehalogenase domain
- P-type ATPase, A domain
- P-type ATPase actuator domain
- P-type ATPase, cytoplasmic domain N
- P5A-type ATPase
- P5A-ATPase, transmembrane helical hairpin
- P5A-ATPase, transmembrane helical hairpin
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ATP13A1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ATP13A1 as an antibody target. Whether an autoantibody or antibody against ATP13A1 could matter depends on whether native ATP13A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATP13A1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label ATP13A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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